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Neurology. Genetics|April 12, 2016
Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutationFábio A Nascimento, Felippe Borlot, Patrick Cossette, et al.Neurology. Genetics|April 12, 2016
LGMD phenotype due to a new gene and dysferlinopathy investigated by next-generation sequencingCorrado I AngeliniNeurology. Genetics|April 12, 2016
White matter lesions in FTLD: distinct phenotypes characterize GRN and C9ORF72 mutationsFatima Ameur, Olivier Colliot, Paola Caroppo, et al.Neurology. Genetics|June 9, 2016
Screening for novel hexanucleotide repeat expansions at ALS- and FTD-associated lociFang He, Julie M Jones, Claudia Figueroa-Romero, et al.Neurology. Genetics|April 12, 2016
A lot of nexts: Next-generation sequencing, databases, and neurologistsStefan M PulstNeurology. Genetics|April 12, 2016
Next-generation sequencing still needs our generation's cliniciansA Reghan Foley, Sandra Donkervoort, Carsten G BönnemannNeurology. Genetics|April 12, 2016
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 lossAshley P L Marsh, Vesna Lukic, Kate Pope, et al.Neurology. Genetics|April 12, 2016
Epileptic spasms are a feature of DEPDC5 mTORopathyGemma L Carvill, Douglas E Crompton, Brigid M Regan, et al.Pageof 85